![](/img/cover-not-exists.png)
Intronic splicing mutations inPTCH1cause Gorlin syndrome
Bholah, Zaynab, Smith, Miriam J., Byers, Helen J., Miles, Emma K., Evans, D. Gareth, Newman, William G.Volume:
13
Language:
english
Journal:
Familial Cancer
DOI:
10.1007/s10689-014-9712-9
Date:
September, 2014
File:
PDF, 333 KB
english, 2014